Variant report

rSNPs within LD-proxies of this variant (count:38)

rs_ID	r²[population]
rs13203375	0.82[EUR][1000 genomes]
rs13208173	0.82[EUR][1000 genomes]
rs13212421	1.00[ASN][1000 genomes]
rs13216754	0.82[EUR][1000 genomes]
rs13217105	0.94[ASN][1000 genomes]
rs13217280	0.82[EUR][1000 genomes]
rs13220611	0.82[EUR][1000 genomes]
rs1361725	0.85[ASN][1000 genomes]
rs1482881	0.98[ASN][1000 genomes]
rs227826	0.98[ASN][1000 genomes]
rs34438627	0.82[EUR][1000 genomes]
rs34747642	0.82[EUR][1000 genomes]
rs34948307	0.82[EUR][1000 genomes]
rs35202871	0.82[EUR][1000 genomes]
rs35270964	0.82[EUR][1000 genomes]
rs35440274	0.82[EUR][1000 genomes]
rs35591728	0.82[EUR][1000 genomes]
rs35939753	0.82[EUR][1000 genomes]
rs36010714	0.82[EUR][1000 genomes]
rs36092281	0.82[EUR][1000 genomes]
rs56780396	0.82[EUR][1000 genomes]
rs58195789	0.86[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs58953717	0.85[ASN][1000 genomes]
rs61014575	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs67120049	0.85[ASN][1000 genomes]
rs67220021	0.97[ASN][1000 genomes]
rs6904819	0.95[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6905076	0.82[EUR][1000 genomes]
rs6905326	0.82[EUR][1000 genomes]
rs6905757	0.82[EUR][1000 genomes]
rs6910103	0.98[ASN][1000 genomes]
rs6915967	0.98[ASN][1000 genomes]
rs6921829	0.94[ASN][1000 genomes]
rs6923447	0.82[EUR][1000 genomes]
rs6936338	0.85[ASN][1000 genomes]
rs71564626	0.82[EUR][1000 genomes]
rs71564627	0.82[EUR][1000 genomes]
rs7770230	0.95[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:1 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1817071	chr6:44670110-44698829	Enhancers Bivalent Enhancer Weak transcription ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:44667200-44691000	Weak transcription	Right Atrium	heart
2	chr6:44670400-44679600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr6:44679400-44681200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr6:44679400-44683600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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